共 50 条
The inhibitory effect of Gleditsia sinensis on cyclooxygenase-2 expression in human esophageal squamous cell carcinoma
被引:18
|作者:
Pak, K. C.
[1
,2
,3
]
Lam, K. Y.
[4
]
Law, S.
[5
]
Tang, J. C. O.
[1
,2
,3
]
机构:
[1] Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Hong Kong, Hong Kong, Peoples R China
[2] Hong Kong Polytech Univ, Lo Ka Chung Ctr Nat Anticanc Drug Dev, Hong Kong, Hong Kong, Peoples R China
[3] Hong Kong Polytech Univ, State Key Lab Chinese Med & Mol Pharmacol, Hong Kong, Hong Kong, Peoples R China
[4] Griffith Univ, Griffith Med Sch, Nathan, Qld 4111, Australia
[5] Univ Hong Kong, Dept Surg, Hong Kong, Hong Kong, Peoples R China
关键词:
esophageal squamous cell carcinoma;
gene overexpression;
cyclooxygenase-2;
anti-proliferation;
NONSTEROIDAL ANTIINFLAMMATORY DRUGS;
FRUIT EXTRACT;
COX-2;
INHIBITORS;
CHINESE ORIGIN;
CANCER;
APOPTOSIS;
OVEREXPRESSION;
ESTABLISHMENT;
PREVENTION;
LINES;
D O I:
10.3892/ijmm_00000109
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
The anti-cancer effects of the anomalous fruit extract of Gleditsia sinensis (GSE) attributed to its apoptotic activity, telomerase inhibition and anti-angiogenesis in a panel of solid and non-solid tumor cell lines including esophageal squamous cell carcinoma (ESCC) have been intensively investigated by us in previous studies. Cyclooxygenase-2 (COX-2) has been well described as another promising target of cancer therapy for ESCC, and novel therapeutic agents are still being sought which target COX-2 expression. However, the anti-cancer effect of GSE through the suppression of COX-2 expression has not been previously investigated. In the present study, the anti-cancer effects of GSE on eight ESCC cell lines (KYSE 30, KYSE 150, KYSE 450, KYSE 510, KYSE 520, HKESC-3, HKESC-4 and SLMT-1) of Chinese and Japanese origins were first studied by MTS cytotoxicity assays. The effects of GSE on COX-2 expression levels and on the housekeeping form COX-1 were also investigated by multiplex RT-PCR analysis. Moreover, the anti-proliferative effect of GSE on KYSE 510 was also studied by anchorage-independent clonogenicity assay in soft agar. The results showed that GSE induced a dose- and time-dependent cytotoxicity on all of the eight ESCC cell lines and caused positive anti-proliferative action on KYSE 510 in the anchorage-independent clonogenicity assay, suggesting that GSE suppressed the in vitro growth of the ESCC cell lines. More importantly, the MRNA expression levels of COX-2, but not COX-1, in all of the ESCC cell lines were suppressed by GSE in a dose-dependent fashion. The overall results of the present study show that the anti-cancer effect of GSE on the ESCC cell lines is associated with the suppression of COX-2 expression, but not COX-L Our findings also open a new chapter for the future advancement of GSE as a novel anticancer agent or as an adjuvant of traditional cancer treatments.
引用
收藏
页码:121 / 129
页数:9
相关论文